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Effect of Ambroxol in Diabetic Peripheral Neuropathy

Primary Purpose

Diabetic Neuropathy Peripheral

Status
Not yet recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Ambroxol Oral Product
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Neuropathy Peripheral focused on measuring Diabetic Complications, Diabetic Peripheral Neuropathy, Inflammatory markers, Tumor necrosis alpha, nuclear factor kappa-light-chain-enhancer of activated B cells, Oxidative stress, Superoxide dismutase

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 18-75 years diagnosed with Type 2 Diabetes.
  • Patients diagnosed with Peripheral Diabetic Neuropathy.

Exclusion Criteria:

  • Patients with autoimmune disorders (Sjogren's syndrome, lupus, rheumatoid arthritis),inherited disorders causing PN (Charcot-Marie-Tooth), thyroid diseases, patients undergone gastroplasty surgery and cancer patients.
  • Pressure on or injury to the nerves
  • Patients with severe kidney or liver dysfunction.
  • Patients with recent history of / or ongoing infection.
  • Patients with cerebral vascular disease, vasculitis, peripheral arterial disease or claudication symptoms, toxic neuritis, vitamin B12 or folate deficiency, spondyloarthropathy, foot edema or ulcer and diagnosis of other neuromuscular disorders or neurodegenerative diseases.
  • Use of medications or supplements known to cause peripheral neuropathy.
  • Patients consuming alcohol, any antioxidant supplements or anti-inflammatory medicines and drug abuse.
  • Ketoacidosis or hypoglycemia resulting in hospital admission within the last 3 months.
  • Pregnancy or lactation or expecting to get pregnant during the study.
  • Medical, psychological, behavioral or pharmacological factors interfering with ability to participate in trial, collection or interpretation of study data.
  • Allergy to ambroxol.

Sites / Locations

  • Ain Shams university Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Ambroxol (intervention arm)

Control arm

Arm Description

40 patients will receive conventional therapy for diabetic neuropathy in addition to ambroxol 450 mg/day divided into 3 doses (each dose consists of 2 75mg capsules) daily for 3 months.

40 patients will receive conventional therapy for diabetic neuropathy for 3 months.

Outcomes

Primary Outcome Measures

Effect of Ambroxol on Tumor necrosis factor alpha (TNF-α)
Blood samples will be drawn at baseline and end of study to track changes in TNF-α using ELISA technique
Effect of Ambroxol on NF-κB (or NF-kappaB, "nuclear factor kappa-light-chain-enhancer of activated B cells")
Blood samples will be drawn at baseline and end of study to track changes in NF-kappaB levels using ELISA technique
Effect of Ambroxol on Superoxide dismutase
Blood samples will be drawn at baseline and end of study to track changes in Superoxide dismutase levels using spectrophotometric technique

Secondary Outcome Measures

Effect of Ambroxol on clinical outcome : Toronto clinical scoring systems (TCSS)
Patient are going to be followed up every other week for detection of progression and severity of neuropathy.
Effect of Ambroxol on clinical outcome : Michigan diabetic neuropathy score (MDNS)
Patient are going to be followed up every other week for detection of progression and severity of neuropathy.
Effect of Ambroxol on clinical outcome : Pain assessment using the Numeric rating scale NRS
Patients are going to be followed up every other week to detect point decrease on pain scale

Full Information

First Posted
September 21, 2022
Last Updated
September 27, 2022
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT05558878
Brief Title
Effect of Ambroxol in Diabetic Peripheral Neuropathy
Official Title
Effect of Ambroxol on the Inflammatory Markers and Clinical Outcome of Patients With Diabetic Peripheral Neuropathy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 1, 2022 (Anticipated)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
November 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
A prospective, randomized, controlled study will be conducted at Department of Endocrinology, Faculty of Medicine, Ain Shams University, assessing the efficacy of Ambroxol addition on the clinical outcome and inflammatory markers in Diabetic peripheral neuropathy patients
Detailed Description
All patients presenting to the Endocrinology department, Ain Shams University Hospitals, will be assessed for eligibility as follow: Inclusion criteria: Patients aged 18-75 years diagnosed with Type 2 Diabetes. Patients diagnosed with Peripheral Diabetic Neuropathy. Exclusion criteria: Patients with autoimmune disorders (Sjogren's syndrome, lupus, rheumatoid arthritis),inherited disorders causing PN (Charcot-Marie-Tooth), thyroid diseases, patients undergone gastroplasty surgery and cancer patients. Pressure on or injury to the nerves Patients with severe kidney or liver dysfunction. Patients with recent history of / or ongoing infection. Patients with cerebral vascular disease, vasculitis, peripheral arterial disease or claudication symptoms, toxic neuritis, vitamin B12 or folate deficiency, spondyloarthropathy, foot edema or ulcer and diagnosis of other neuromuscular disorders or neurodegenerative diseases. Use of medications or supplements known to cause peripheral neuropathy. Patients consuming alcohol, any antioxidant supplements or anti-inflammatory medicines and drug abuse. Ketoacidosis or hypoglycemia resulting in hospital admission within the last 3 months. Pregnancy or lactation or expecting to get pregnant during the study. Medical, psychological, behavioral or pharmacological factors interfering with ability to participate in trial, collection or interpretation of study data. Allergy to ambroxol. Eligible patients will be randomly assigned to one of 2 groups: Group 1, Ambroxol group (n=40): Patients will receive conventional therapy for diabetic neuropathy in addition to ambroxol 450 mg/day divided into 3 doses (each dose consists of two 75mg tablets) daily for 3 months. Group 2, Control group (n= 40): Patients will receive conventional therapy for diabetic neuropathy for 3 months. All subjects will sign an informed consent statement prior to inclusion in the study. Follow up evaluation : All patients in both groups will be followed up every other week & will be assessed for the following: Diabetic neuropathy scoring, occurrence of side effects & Pain assessment. End of study evaluation : After 3 months, all patients will be assessed for the same parameters assessed at baseline.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Neuropathy Peripheral
Keywords
Diabetic Complications, Diabetic Peripheral Neuropathy, Inflammatory markers, Tumor necrosis alpha, nuclear factor kappa-light-chain-enhancer of activated B cells, Oxidative stress, Superoxide dismutase

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ambroxol (intervention arm)
Arm Type
Experimental
Arm Description
40 patients will receive conventional therapy for diabetic neuropathy in addition to ambroxol 450 mg/day divided into 3 doses (each dose consists of 2 75mg capsules) daily for 3 months.
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
40 patients will receive conventional therapy for diabetic neuropathy for 3 months.
Intervention Type
Drug
Intervention Name(s)
Ambroxol Oral Product
Intervention Description
Drug: Ambroxol (75 mg capsule) Ambroxol is a mucolytic and expectorant drug. Ambroxol has been approved as lozenges for topical analgesia of sore throat in pharyngitis owing to its local anesthetic properties. Anti-inflammatory properties of ambroxol were confirmed by numerous studies. Ambroxol affect neuronal transduction by blocking (TTX)-resistant Na+ channels (Nav1.8) in small (pain-sensing) dorsal root ganglion neurons more potently than TTX-sensitive channels.
Primary Outcome Measure Information:
Title
Effect of Ambroxol on Tumor necrosis factor alpha (TNF-α)
Description
Blood samples will be drawn at baseline and end of study to track changes in TNF-α using ELISA technique
Time Frame
3 months
Title
Effect of Ambroxol on NF-κB (or NF-kappaB, "nuclear factor kappa-light-chain-enhancer of activated B cells")
Description
Blood samples will be drawn at baseline and end of study to track changes in NF-kappaB levels using ELISA technique
Time Frame
3 months
Title
Effect of Ambroxol on Superoxide dismutase
Description
Blood samples will be drawn at baseline and end of study to track changes in Superoxide dismutase levels using spectrophotometric technique
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Effect of Ambroxol on clinical outcome : Toronto clinical scoring systems (TCSS)
Description
Patient are going to be followed up every other week for detection of progression and severity of neuropathy.
Time Frame
3 months
Title
Effect of Ambroxol on clinical outcome : Michigan diabetic neuropathy score (MDNS)
Description
Patient are going to be followed up every other week for detection of progression and severity of neuropathy.
Time Frame
3 months
Title
Effect of Ambroxol on clinical outcome : Pain assessment using the Numeric rating scale NRS
Description
Patients are going to be followed up every other week to detect point decrease on pain scale
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 18-75 years diagnosed with Type 2 Diabetes. Patients diagnosed with Peripheral Diabetic Neuropathy. Exclusion Criteria: Patients with autoimmune disorders (Sjogren's syndrome, lupus, rheumatoid arthritis),inherited disorders causing PN (Charcot-Marie-Tooth), thyroid diseases, patients undergone gastroplasty surgery and cancer patients. Pressure on or injury to the nerves Patients with severe kidney or liver dysfunction. Patients with recent history of / or ongoing infection. Patients with cerebral vascular disease, vasculitis, peripheral arterial disease or claudication symptoms, toxic neuritis, vitamin B12 or folate deficiency, spondyloarthropathy, foot edema or ulcer and diagnosis of other neuromuscular disorders or neurodegenerative diseases. Use of medications or supplements known to cause peripheral neuropathy. Patients consuming alcohol, any antioxidant supplements or anti-inflammatory medicines and drug abuse. Ketoacidosis or hypoglycemia resulting in hospital admission within the last 3 months. Pregnancy or lactation or expecting to get pregnant during the study. Medical, psychological, behavioral or pharmacological factors interfering with ability to participate in trial, collection or interpretation of study data. Allergy to ambroxol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Beshoy Thabet, Bachelor of Pharmacy
Phone
+20 1111058017
Email
beshoy.thabit@pharma.asu.edu.eg
Facility Information:
Facility Name
Ain Shams university Hospital
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
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Effect of Ambroxol in Diabetic Peripheral Neuropathy

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